Canonical Allele Identifier: CA2706485217
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs2149326494

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404406_73404407insACAAGA , CM000666.2:g.73404406_73404407insACAAGA GRCh38
NC_000004.11:g.74270123_74270124insACAAGA , CM000666.1:g.74270123_74270124insACAAGA GRCh37
NC_000004.10:g.74488987_74488988insACAAGA NCBI36
NG_009291.1:g.5152_5153insACAAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.79_79+1insACAAGA MANE Select ENSP00000295897.4:n.79_79+1insACAAGA
ENST00000295897.8:c.79_79+1insACAAGA ENSP00000295897.4:n.79_79+1insACAAGA
ENST00000401494.7:c.79_79+1insACAAGA ENSP00000384695.3:n.79_79+1insACAAGA
ENST00000415165.6:c.79_79+1insACAAGA ENSP00000401820.2:n.79_79+1insACAAGA
ENST00000441319.5:c.85_85+1insACAAGA ENSP00000392541.1:n.85_85+1insACAAGA
ENST00000476441.6:c.79_79+1insACAAGA ENSP00000423727.1:n.79_79+1insACAAGA
ENST00000503124.5:c.-102_-102+1insACAAGA ENSP00000421027.1:n.-102_-102+1insACAAGA
ENST00000509063.5:c.79_79+1insACAAGA ENSP00000422784.1:n.79_79+1insACAAGA
ENST00000510166.5:n.120_120+1insACAAGA
ENST00000514786.1:n.48+70_48+71insACAAGA
ENST00000515133.5:n.120_120+1insACAAGA
ENST00000621085.4:c.79_79+1insACAAGA ENSP00000483421.1:n.79_79+1insACAAGA
ENST00000621628.4:c.79_79+1insACAAGA ENSP00000480485.1:n.79_79+1insACAAGA
NM_000477.5:c.79_79+1insACAAGA NP_000468.1:n.79_79+1insACAAGA
NM_000477.6:c.79_79+1insACAAGA NP_000468.1:n.79_79+1insACAAGA
NM_000477.7:c.79_79+1insACAAGA MANE Select NP_000468.1:n.79_79+1insACAAGA